Evidence map›Paper›PMID 29864442›Full record

ReviewJournal of molecular biology2018

Regulation of Polarity Protein Levels in the Developing Central Nervous System.

Christophe Laumonnerie, David J Solecki

Abstract readReview
In one paragraph

Review in Journal of molecular biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Integrative Analysis of Key Signalling Pathways in Neural Tube Defects: From Molecular Mechanisms to Therapeutic Strategies.International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Christophe LaumonnerieDepartment of Developmental Neurobiology, St Jude Children's Research Hospital, 262 Danny Thomas Blvd, Memphis, TN 38105, USA.
David J SoleckiDepartment of Developmental Neurobiology, St Jude Children's Research Hospital, 262 Danny Thomas Blvd, Memphis, TN 38105, USA. Electronic address: David.Solecki@stjude.org.

Funding

Polarity Signals Coordinate Neuronal Migration and Germinal Zone ExitR01NS066936 · NINDS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SOLECKI, DAVID JOSEPH · 2011 to 2021
$3.9M
Siah2: an E3 ligase organizes polarity and cytoskeletal links in neuron migrationR01NS104029 · NINDS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SOLECKI, DAVID JOSEPH · 2018 to 2022
$2.0M
NINDS NIH HHS R01 NS066936NINDS NIH HHS R01 NS104029
6 · The paper itself

Abstract

In the course of their development from neuroepithelial cells to mature neurons, neuronal progenitors proliferate, delaminate, differentiate, migrate, and extend processes to form a complex neuronal network. In addition to supporting the morphology of the neuroepithelium and radial glia, polarity proteins contribute to the remodeling of processes and support the architectural reorganizations that result in axon extension and dendrite formation. While a good amount of evidence highlights a rheostat-like regulation by signaling events leading to local activation and/or redistribution of polarity proteins, recent studies demonstrate a new paradigm involving a switch-like regulation directly controlling the availability of polarity protein at specific stage by transcriptional regulation and/or targeted ubiquitin proteasome degradation. During the process of differentiation, most neurons will adopt a morphology with reduced polarity which suggests that polarity complex proteins are strongly repressed during key step of development. Here we review the different mechanisms that directly impact the levels of polarity complex proteins in neurons in relation to the polarization context and discuss why this transient loss of polarity is essential to understand neural development and how this knowledge could be relevant for some neuropathy.

Indexed as

AnimalsCell PolarityCentral Nervous SystemEpithelial-Mesenchymal TransitionHumansNerve Tissue ProteinsNeuronsProtein Processing, Post-TranslationalNerve Tissue ProteinsneuronPard3polarity protein

Identifiers

PMID29864442
PMCPMC6783131

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.